31679-13-7Relevant articles and documents
Are multicomponent strecker reactions of diketones with diamines under high pressure amenable to heterocyclic synthesis?
Kumamoto, Koji,Iida, Hirokazu,Hamana, Hiroshi,Kotsuki, Hiyoshizo,Matsumoto, Kiyoshi
, p. 675 - 681 (2007/10/03)
Employing double Strecker strategy, two new heterocyclic compounds, 5,6,11,12-tetrahydro-6,11-dimethyldibenzo[b,f][1,4]diazocine-6,11-dicarbonitrile and 1,2,3,4,5,10-hexahydrophenazine-4a, 10a-dicarbonitrile, were prepared in one step albeit in low yields. The reaction has proven to be very limited, but such a sterically hindered amine as N-methylaniline underwent Strecker reaction with benzaldehyde and TMSCN to give the corresponding α-amino nitriles.
Synthesis of fluoroorganic O-(Trirnethylsilyl)cyanhydrines
Sander, Michael,Sundermeyer, Wolfgang
, p. 296 - 306 (2007/10/03)
Fluororganic and/or sterically hindered cyanohydrines are useful synthetic reagents, not readily available directly from e.g. aldehydes or ketones and hydrogen cyanide. By using trimethylsilyl cyanide (TMSCN), the obtained O-Silyl-cyanohydrines can be app